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“Something Smells… Fishy”: The Use of Smell in Genetic Diagnoses

June 2, 2017 Morgan Simmons, MMSc, CGC 4 Comments

Use of Smell in Genetic Diagnoses

Genetic diseases can be diagnosed using a variety of methods: physical exam, personal/family medical history, or tests performed in a laboratory.  But, did you know that smells can also be… CONTINUE

Filed Under: Education Tagged With: genetic condition, getting diangosed, Isovaleric acidemia, maple syrup urine disease, Morgan Simmons, MSUD, olfactory receptors, PAH, Phenylketonuria, PKU, TMA, TMAU, Trimethylamiruria

Genetic Condition Update for Week of 03/31/2017

March 31, 2017 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: Fetal parvovirus, Hereditary hemorrhagic telangiectasia, HHT, Long-chain 3-hydroxyacyl-coa dehydrogenase deficiency, Lynch syndrome, Phenylketonuria, ThinkGenetic, tyrosinemia type 1, update

Weekly Site Update for 10/03/2016

October 3, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: achondrogensis, Alpha-thalassemia, Andersen-Tawil Syndome, attention deficits, birth defects, Cardiofaciocutaneous syndrome, Congenital insensitivity to pain, cysts, Duchenne and becker muscular dystrophy, Familial adenomatous polyposis, GM2, hemangioblastomas, Hemophilia A, Hemophilia B, Hypophosphatasia, Lysosomal acid lipase deficiency, mood disorders, neurological, Phenylketonuria, Prader-willi syndrome, Roberts syndrome, Sotos syndrome, SYNGAP1, Tay-Sachs, tumors, VHL, Von Hippel-Lindau

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